LSC have a great contract opportunity for a Sr Document Controller to join the client project team on a major Dublin based Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.
The role is fully embedded on site and responsible for the client-side control and governance of all project documentation across design, construction, CQV and handover phases.
If you are an experienced Document Controller with 5 + years experience in a similar role this could be the next contract for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
· Client-side control of all project documentation across the full lifecycle
· Manage document receipt, review, approval, issue, revision control and archiving
· Interface with EPCM partners, vendors, contractors and internal stakeholders
· Ensure documentation complies with GMP, data integrity and ALCOA+ principles
· Maintain accurate document registers, trackers and status reports
· Support CQV documentation, executed protocols and final turnover to operations
· Support audits, inspections and project close-out activities
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
· Proven experience as a Document Controller on pharmaceutical or life sciences capital projects
· Essential: hands-on experience using EIDA for document management
· Experience working client-side or within an owner's project team
· Strong understanding of GMP documentation requirements
· Experience supporting construction, commissioning and qualification documentation
· Ability to work full-time on a live pharmaceutical site in Ireland
Desirable
· Experience on large-scale Irish pharma projects (drug product, biologics, sterile facilities)
· Familiarity with ValGenesis, Kneat, ACC or similar platforms
Apply via this advert or contact Kathy Gillen on 021 4777329 if you have any more questions about this role!
